What this is
- This analysis examines cardiovascular outcomes associated with sodium-glucose cotransporter-2 inhibitors (SGLT-2i) compared to other glucose-lowering drugs (oGLD).
- Data from 440,599 patients across 13 countries were analyzed to assess risks of hospitalization for heart failure, all-cause death, myocardial infarction, and stroke.
- The study aims to provide insights into the effectiveness of SGLT-2i in a diverse, real-world population, extending findings from prior clinical trials.
Essence
- Initiation of SGLT-2i is linked to lower risks of heart failure, all-cause death, myocardial infarction, and stroke compared to oGLD. These findings are consistent across various patient subgroups and geographic regions.
Key takeaways
- SGLT-2i initiation is associated with a 34% lower risk of hospitalization for heart failure (: 0.66). This finding supports the effectiveness of SGLT-2i in reducing heart failure events.
- SGLT-2i initiation results in a 48% lower risk of all-cause death (: 0.52). This significant reduction underscores the potential of SGLT-2i in improving overall survival in patients with type 2 diabetes.
- The composite outcome of hospitalization for heart failure or all-cause death shows a 40% lower risk with SGLT-2i (: 0.60). This suggests that SGLT-2i may provide a dual benefit in managing cardiovascular risks.
Caveats
- Despite robust statistical methods, residual confounding may affect results. Important patient-level data were not available for some countries, potentially limiting generalizability.
- The analysis primarily includes high-income countries, which may not reflect outcomes in lower-income populations. Safety comparisons between SGLT-2i and oGLD were not assessed.
Definitions
- SGLT-2 inhibitors: A class of medications used to lower blood sugar levels in patients with type 2 diabetes by preventing glucose reabsorption in the kidneys.
- hazard ratio (HR): A measure used to compare the risk of an event occurring in two different groups over time.
Simplified
Background
Despite recent improvements, cardiovascular disease (CVD) remains the leading global cause of mortality and morbidity in patients with type 2 diabetes [1]. The prevalence of diabetes continues to increase, with the majority of people affected residing in the Asia–Pacific region, South East Asia and the Middle East [2–4]. However, global outcomes data are sparse for new therapies in people with type 2 diabetes, especially outside North America and Europe. Previous studies have shown large variations in the management of people with diabetes and the prevalence of complications [5, 6]. More recently, global collaborative studies have shown that there are differences in patient characteristics, treatment patterns, and types of adverse CVD events experienced by patients in different regions and different ethnicities [7]. Moreover, results of randomized controlled cardiovascular outcome trials have been criticised for not being representative of the management of people with type 2 diabetes in real-world settings [8], with most patients being recruited in North America and Europe. Clinicians across other world regions are therefore cautious about generalizing the results of trials into their clinical practice.
Over recent years, there has been a number of studies reporting the comparative effectiveness of novel therapies in the ‘real-world’ setting. Sodium–glucose cotranspoter-2 inhibitors (SGLT-2is) have now been studied in several cardiovascular outcome trials [9–13], with a recent systematic review and meta-analysis showing the benefits of this class of drugs on major cardiovascular events in people with established CVD, and on heart failure and renal outcomes in people with and without CVD [14]. We have previously conducted a number of pharmaco-epidemiological studies (CVD-REAL—Comparative Effectiveness of Cardiovascular Outcomes in New Users of Sodium–Glucose Cotransporter-2 Inhibitors) on the effectiveness of SGLT-2i in the real-world setting [15, 16]. Although there were differences in point estimates across countries for some outcomes, the directionality of associations was consistent despite variable patient characteristics, health care settings, practice patterns, and specific SGLT-2i compounds used.
In this study, we conducted further analyses of the largest CVD-REAL dataset to date, to assess a broad range of cardiovascular outcomes, including hospitalization for heart failure, all-cause mortality, myocardial infarction, and stroke. Our additional aim was to use the large number of patients and events in this dataset to expand the results of CVD-REAL by examining SGLT2i effects across a broad range of subgroups including baseline therapies and other chronic multimorbidities. We also report on the time trends of SGLT-2i prescribing in the 13 included countries.
Methods
Data sources
Analyses were conducted on de-identified health records from 13 countries (Australia, Canada, Denmark, Finland, Germany, Israel, Japan, Singapore, South Korea, Spain, Sweden, Taiwan, and the USA). Descriptions of the sources of data have been reported previously [16–19], apart from Finland which is included in Additional file: Data Sources 1.
Patient cohort
Patients with type 2 diabetes were identified using standard diagnosis codes (Additional file: Table S1), except in Australia where this was based on physician or nurse educator clinical diagnosis of type 2 diabetes. All episodes of new initiation of either SGLT-2i or other glucose-lowering drugs (oGLD) were selected within the country-specific date range for availability of SGLT-2i [Additional file: Table S2; range: December 1, 2012 (Denmark) to May 1, 2016 (Taiwan)]. Treatment initiation episodes were defined as written/dispensed prescription (as initial or add-on therapy) for any SGLT-2i or oGLD, including fixed-dose combinations, without any use of the same therapy during the preceding 12 months; a patient might contribute with several episodes, every time the criteria of new user is met. Additional inclusion criteria were: age ≥ 18 years on the index date (defined as the prescription date for new initiation of an SGLT-2i or oGLD) and availability of historic data for more than 1 year in the database before the index date. Patients with type 1 or gestational diabetes were excluded. Patients were followed from the index date until migration/leaving the practice/database, last date of data collection, outcome date, or censoring date [Additional file: Table S2; range: December 31, 2014 (Australia) to November 30, 2017 (Singapore)]. 1 1 1
Outcomes
The outcomes were hospitalization for heart failure (HHF), all-cause death, the composite of HHF or all-cause death, non-fatal myocardial infarction, or non-fatal stroke. Outcomes were defined using primary discharge diagnosis codes (Additional file 1: Table S3) and validated independently in each country. Data regarding all-cause death were available from all countries; data for the other outcomes were available from all countries except Australia. Additionally, in Japan and Singapore only information on in-hospital deaths was available; however, in-hospital deaths represent the majority of fatal events in these countries according to the national statistics [20, 21]. In Sweden and Denmark, HHF was defined by any hospital visit with a registered main diagnosis of heart failure [inpatient or outpatient visit; defined using diagnosis codes (Additional file 1: Table S3)].
Statistical analysis
Detailed statistical methods are described in a prior publication [15]. Briefly, baseline characteristics were analyzed using descriptive statistics. Categorical variables were described by frequencies and percentages, and mean ± standard deviation (SD) were used for continuous variables. The overall mean across all databases was a summary estimate of country-specific means, weighted according to the number of patients in each database. The proportion of exposure time contributed by individual agents was summarized both overall and by country.
A non-parsimonious propensity score for initiating SGLT-2i was developed separately for each country. All available variables in each country that could affect treatment assignment or outcomes were included in the propensity score (Additional file 1: Table S4; baseline comorbidity information was not available for Australia, although extensive medication data were available). Based on propensity scores, episodes of patients initiating SGLT-2i were matched 1:1 with episodes of initiating oGLD. The adequacy of matching was assessed by evaluating post-match standardized differences in patient characteristics (Table 1). A non-negligible imbalance was considered if a > 10% standardized difference occurred between the two groups post-match.
The incidence rate (IR) for each outcome was assessed by treatment group as the number of events divided by the total number of person-years at risk. The time to first event was compared between groups using Cox proportional hazards models, presented as hazard ratios (HR; 95%CI) for each outcome separately by country. The primary analysis used an intent-to-treat (ITT) approach where patients were followed from the start of index treatment until either occurrence of the first outcome event or the censoring date (whichever came first), regardless of whether index treatment was discontinued. The HRs for each endpoint from each individual country were then pooled for an overall weighted summary [22], using random-effects models with inverse variance weighting for each country [23].
Analyses for each outcome were also stratified according to the presence of prior CVD [defined as history of myocardial infarction, unstable angina, heart failure, atrial fibrillation, stroke, percutaneous coronary intervention (PCI) or coronary artery bypass graft (CABG)]; patient age and sex; history of heart failure, chronic kidney disease (CKD), or cancer; baseline use of angiotensin-converting enzyme inhibitors (ACEi) or angiotensin receptor blockers (ARBs), β-blockers, high ceiling diuretics, aldosterone antagonists, insulin, sulphonylureas, and statins.
Sensitivity analyses were performed in order to evaluate the stability of the findings: data for the primary analysis were additionally adjusted for multiple covariates [age, gender, frailty (defined as at least one hospitalization of at least three consecutive days during the year prior to index), history of heart failure, history of myocardial infarction, atrial fibrillation history, hypertension (if available), obesity/BMI (if available), duration of diabetes (if available), and use of ACEi or ARBs, β-blockers, Ca2+-channel blockers, statins, loop diuretics and thiazide diuretics]; analyses were repeated using an on-treatment approach (follow-up censored at index treatment discontinuation).
Informed consent was not required, as the data were collected for clinical and administrative purposes and were analysed after de-identification. Analyses of data were conducted in accordance with local laws and regulations, and received approvals from Scientific/Ethics/Data Protection Committees in each country. Country-specific analyses were conducted by independent academic/statistical groups in each country. Meta-analyses were conducted by Statisticon AB, Uppsala (Sweden) and validated by independent academic statisticians at Saint Luke’s Mid America Heart Institute, Kansas City, Missouri (USA).
| SGLT-2 inhibitor (N = 440,599) | oGLD (N = 440,599) | std diff (%) | |
|---|---|---|---|
| Age, years | 58.0 (11.6) | 57.8 (12.7) | 1.4 |
| Women | 193,825 (44.0) | 194,123 (44.1) | 0.1 |
| CV-history | 134,331 (31.5) | 129,993 (30.5) | 2.2 |
| Myocardial infarction | 19,346 (4.5) | 18,968 (4.4) | 0.4 |
| Unstable angina | 22,030 (5.2) | 21,489 (5.0) | 0.6 |
| Heart failure | 32,736 (7.7) | 31,948 (7.5) | 0.7 |
| Atrial fibrillation | 18,448 (4.3) | 17,910 (4.2) | 0.6 |
| Stroke | 47,437 (11.1) | 45,353 (10.6) | 1.6 |
| PAD | 22,391 (5.2) | 22,054 (5.2) | 0.4 |
| Microvascular disease | 218,288 (51.1) | 214,311 (50.2) | 1.9 |
| CKD | 24,528 (5.7) | 23,969 (5.6) | 0.6 |
| Frailty (yes)* | 36,736 (8.9) | 36,498 (8.8) | 0.2 |
| Glucose-lowering therapies | |||
| Metformin | 334,441 (75.9) | 335,731 (76.2) | 0.7 |
| SU | 197,712 (44.9) | 197,117 (44.7) | 0.3 |
| DPP-4i | 205,550 (46.7) | 203,469 (46.2) | 0.9 |
| TZD | 48,775 (11.1) | 46,710 (10.6) | 1.5 |
| GLP-1RA | 36,903 (8.4) | 34,033 (7.7) | 2.4 |
| Insulin | 109,470 (24.8) | 104,973 (23.8) | 2.4 |
| Anti-hypertensive therapy | 308,944 (70.1) | 304,417 (69.1) | 2.2 |
| Loop diuretics | 38,852 (8.8) | 37,785 (8.6) | 0.9 |
| Low ceiling diuretics | 54,358 (12.3) | 53,731 (12.2) | 0.4 |
| ACEi | 97,176 (22.1) | 97,019 (22.0) | 0.1 |
| ARBs | 183,048 (41.5) | 181,136 (41.1) | 0.9 |
| Statin therapy | 288,674 (65.5) | 286,787 (65.1) | 0.9 |
| Beta blockers | 114,079 (25.9) | 112,092 (25.4) | 1 |
| Aldosterone antagonists | 14,215 (3.2) | 13,998 (3.2) | 0.3 |
| Index year | |||
| 2012 | 20 (0.0) | 109 (0.1) | 2.6 |
| 2013 | 12,006 (5.5) | 11,889 (5.4) | 0.2 |
| 2014 | 64,187 (16.2) | 63,126 (15.9) | 0.7 |
| 2015 | 120,957 (30.8) | 121,370 (30.9) | 0.2 |
| 2016 | 206,590 (49.3) | 205,948 (49.2) | 0.3 |
| 2017 | 36,839 (20.7) | 38,157 (21.4) | 1.8 |
Role of funding source
This analysis was overseen by the CVD-REAL (Comparative Effectiveness of Cardiovascular Outcomes in New Users of Sodium–Glucose Cotransporter-2 Inhibitors) Academic Scientific Committee, Study Group and Investigators, including members from the sponsor. The sponsor was involved in the design of the analysis, and the collection/interpretation of data. No payment was received by any author for writing this manuscript. The corresponding author and senior author had full access to all data, and vouch for the accuracy and completeness of data reported. All authors made the final decision to submit the manuscript.
Results
Study population
A total of 9,631,497 patients who newly initiated either SGLT-2i or oGLD treatment during the study period was identified (Additional file: Figure S1); 477,894 (5.0%) were new users of SGLT-2i and 9,153,603 (95.0%) were new users of oGLD. Prior to propensity score matching, the patients who initiated SGLT-2i were younger, had slightly less prevalent heart failure, stroke and CKD at baseline and greater use of statins, ACEis and low-ceiling diuretics (Additional file: Table S5). Patients initiated on SGLT-2i were also more likely to be receiving other glucose-lowering drugs at baseline (Additional file: Table S5). 1 1 1
Following propensity score matching, there were 440,599 new initiators of SGLT-2i and 440,599 new initiators of oGLDs (Additional file 1: Figure S1) and the baseline characteristics were well-balanced (Table 1). In both groups, the mean age was 58 years, 44% were women, and 31% had established CVD; 65% of patients received statins, 69% antihypertensive medications, and 76% metformin (Table 1). The distribution of specific SGLT-2i compounds initiated is shown in Additional file 1: Table S6; dapagliflozin contributed 60% of total exposure time, followed by canagliflozin (20%) and empagliflozin (14%), with other SGLT-2is providing smaller contributions. The distribution of oGLD by class is shown in Additional file 1: Table S7; the DPP-4i class contributed to 25% of the oGLD exposure time, followed by insulin (18%), SUs (18%), metformin (13%) and TZDs (11%); other classes (GLP-1 RA, acarbose and metiglinides) contributed < 10% each and made up the remainder.
Pre-propensity match, the proportion of new SGLT-2i episodes that were identified for each included country is shown in Fig. 1 as a function of time. For the countries included in this study, the proportion of new initiations that were SGLT-2i increased consistently over time; in North America, the proportion increased until 2015, with a slight decrease thereafter. When all countries included in this analysis were considered together, the proportion of new SGLT-2i initiation increased from around 3% of all new initiations in 2013, to about 15% in 2017 (Fig. 1).
Trends in proportion of new user episodes which were SGLT-2i bycountry andoverall in 2012–2017 (pre-propensity matching).sodium–glucose cotransporter-2 inhibitor A B SGLT-2i
Outcomes
The mean follow-up time for the primary ITT analysis was 396 days for SGLT-2i and 406 days for oGLDs initiations (Additional file: Table S8). 1
During 914,208 patient-years of follow-up there were 9121 events of HHF (3913 in the SGLT-2i group and 5208 in the oGLD group; Additional file 1: Table S9). Initiation of SGLT-2i was associated with a lower risk of HHF (ITT-unadjusted pooled HR: 0.66, 95%CI 0.58–0.75; p < 0.001; Fig. 2). While there was heterogeneity, there were consistent associations between use of SGLT2i and lower risk of heart failure in all of the 13 countries (Additional file 1: Figure S2A).
During 968,452 patient-years of follow-up, there were 10,252 events of all-cause death (3712 in the SGLT-2i group and 6540 in the oGLD group; Additional file 1: Table S9). Initiation of SGLT-2i was associated with a lower risk of all-cause death (ITT-unadjusted pooled HR: 0.52, 95%CI 0.45–0.60; p < 0.001; Fig. 2). While there was heterogeneity, there were consistent associations between use of SGLT2i and lower risk of all-cause death in all of the 13 countries (Additional file 1: Figure S2B).
For the composite outcome of HHF or all-cause death, there were 17,207 events (6932 in the SGLT-2i group and 10,275 in the oGLD group) over 898,869 patient-years of follow-up (Additional file 1: Table S9). Initiation of SGLT-2i was associated with a lower risk of the composite of HHF or all-cause death (ITT-unadjusted pooled HR: 0.60, 95%CI 0.53–0.68; p < 0.001; Fig. 2). While there was heterogeneity, there were consistent associations between use of SGLT2i and lower risk of HHF or all-cause death in all of the 13 countries (Additional file 1: Figure S2C).
For myocardial infarction, there were 4880 events (2203 in the SGLT-2i group and 2677 in the oGLD group) over 916,305 patient-years of follow-up (Additional file 1: Table S9): initiation of SGLT-2i was associated with a lower risk of myocardial infarction (ITT-unadjusted pooled HR: 0.85, 95%CI 0.78–0.92; p < 0.001; Fig. 2; Additional file 1: Figure S2D).
For stroke, there were 9111 events (3981 in the SGLT-2i group and 5130 in the oGLD group) over 913,571 patient-years of follow-up (Additional file 1: Table S9): initiation of SGLT-2i was associated with a lower risk of stroke (ITT-unadjusted pooled HR: 0.78, 95%CI 0.72–0.85; p < 0.001; Fig. 2; Additional file 1: Figure S2E). There was no evidence of treatment heterogeneity across countries for the outcomes of myocardial infarction or stroke (p for interaction > 0.07).
Pooled hazard ratios for the outcomes of hospitalization for heart failure, all-cause death, composite of hospitalization for heart failure or all-cause death, myocardial infarction, and stroke (Intent-to-treat analysis; unadjusted).all-cause death,heart failure,other glucose-lowering drug,patient–years,sodium–glucose cotransporter-2 inhibitor ACD HF oGLD PY SGLT-2i
Subgroup and sensitivity analyses
Analyses of data stratified by baseline characteristics continued to favor SGLT-2is over oGLD for the outcomes of HHF, all-cause death, composite of HHF or all-cause death, myocardial infarction and stroke across all subgroups, with very few significant interactions (Fig. 3).
Findings similar to the primary analyses were seen upon multivariable adjustment and in the on-treatment analyses (Additional file: Figures S3-S5). 1
Pooled hazard ratios forhospitalization for heart failure,all-cause death,composite of hospitalization for heart failure or all-cause death,myocardial infarction, andstroke stratified by subgroups (Intent-to-treat analysis; adjusted). Event rate, events per 100-person years;angiotensin converting enzyme inhibitors,angiotensin receptor blockers,other glucose-lowering drug,sodium–glucose cotransporter-2 inhibitor A B C D E ACE ARB oGLD SGLT-2i
Discussion
In this latest update to the CVD-REAL study, that included nearly 10 million people from 13 countries, we report a number of notable findings. First, we show temporal trends in the prescribing of SGLT-2i therapies across three continents from 2012 to 2017, highlighting large global variations. Second, we show that in an analysis of data from a much larger number of countries and patients than previously reported, initiation of SGLT-2i therapy was associated with significantly lower risk of HHF, all-cause death, composite of HHF or all-cause death, myocardial infarction and stroke, compared with the initiation of oGLDs. Finally, we demonstrate that the clinical benefit of SGLT-2is compared to oGLDs was highly consistent across a number of prespecified subgroups, including age, sex, co-morbidities and use of various cardiovascular and anti-hyperglycemic agents. The results of this study, therefore, extend findings from prior CVD-REAL analyses and from the SGLT-2i inhibitor clinical trials in a broader, more ethnically diverse population from 13 countries.
Despite the significant cardiovascular benefits of SGLT-2i therapy reported in CVOTs and comparative effectiveness studies [10–12, 15, 16, 24–26], previous single country studies have shown that only a small proportion of people meeting the criteria for the CVOTs are prescribed these therapies [27, 28]. The DISCOVER study of 37 countries with 14,668 participants showed that, overall, the prescriptions for SGLT-2i were low during the study period 2014–2016, but also showed variations across continents [29]. In our study, assessment of the prescribing trends in the pre-matched patients from 2012 to 2017 demonstrated that, overall, use of SGLT-2i has increased since 2013, from around 3% of all new initiations in 2013 to about 15% in 2017; although this proportion remains low overall despite the evidence of the benefits of SGLT-2i. There were large variations between countries and over time, with the steepest increases in prescribing of SGLT-2i over this period seen in Canada and Israel. Recent data from the UK has also shown slow but steady increases in prescriptions for SGLT-2i as second-line therapy to metformin from 2014 to 2017 [30].
The populations of the SGLT-2i CVOTs differed in the proportions of patients with established CVD that were recruited. The EMPA-REG, CANVAS Programme and the DECLARE-TIMI 58 trials included 100%, 65.6% and 37.4%, respectively, people with type 2 diabetes and established atherosclerotic CVD, with the remainder having risk factors for CVD [10, 11, 31]. A meta-analysis of these three trials, with 34,322 patients and 3342 major cardiovascular events found that compared to placebo, SGLT-2i reduced major adverse cardiovascular events (cardiovascular death, myocardial infarction or stroke) by around 11% overall (HR 0.89, 95% CI 0.83–0.96), with benefit seen in those with established atherosclerotic CVD [14]. Similarly the meta-analysis also demonstrated a benefit with SGLT-2i against the risk of cardiovascular deaths or HHF (HR 0.77, 95% CI 0.71–0.84), and this benefit was seen across those with and without established CVD [14]. The results from this analysis of the CVD-REAL data, where the proportion of participants with established CVD was much lower at just over 30%, complement the findings from the CVOTs, and are similar to those seen in previous observational studies [24–26], thus further supporting the benefits of SGLT-2i in improving cardiovascular outcomes across a broad patient population. As one would expect, the absolute risks reductions are lower for those without versus with established CVD, yet the relative risk reductions are similar in both groups. The difference in the patient populations included in comparative-effectiveness studies and the CVOTs (where strict inclusion criteria are used), may explain some of the difference in magnitude of benefit seen between these studies.
There are a number of strengths in our study. This is the largest comparative effectiveness study of any glucose-lowering therapy to date with over 880,000 propensity-matched patients from a pooled population from 13 countries with different healthcare systems. Despite a lower cardiovascular risk population, we had a very large number of events in view of the size of the study cohort, allowing adequate power for multiple subgroup analyses. When considering the number of all-cause deaths there were 10,252 events in our study compared to 5216 in CVD-REAL 2; while in the CVOTs there were 463 events in EMPA-REG OUTCOME; 681 events in the CANVAS Programme; and 1099 in the DECLARE-TIMI 58 study [10–12, 15, 16]. This is a major strength of real-world comparative-effectiveness studies, as this large number of events in a broad population would not be feasible in a randomized controlled trial. As with other CVD-REAL studies, we found no geographic heterogeneity in outcomes from the 13 countries with the direction of the association for the benefits for SGLT-2i similar in all countries; and as some countries or regions favor specific agents (such as dapagliflozin in South Korea or canagliflozin the USA) this suggests generally similar effects for SGLT-2is contributing to this study.
These findings should be considered in light of some important limitations. Despite using robust statistical techniques including propensity score matching, the possibility of residual unmeasured confounding cannot be excluded. The data used in this analysis did not include important patientlevel data such as risk factor control, or comprehensive comorbidity data at baseline for some of the countries. In Japan and Singapore only in-hospital deaths were included. However, as most fatal events in these countries occur in hospital [20, 21], and the estimates for the outcomes were directionally similar to the other countries, where capture of the mortality data was more comprehensive, the results for all-cause death in these countries are consistent with our findings in other participating countries. The countries included in this study were all high-income, and therefore these findings may not be applicable to all patient populations. Safety of SGLT-2i versus oGLD was not assessed in our analysis; however, other randomized controlled trials and real-world studies have confirmed the relative safety of the SGLT-2i class [32]. While we included a large numbers of patients, the overall follow-up was relatively short (just over 12 months) given the relatively recent introduction of SGLT-2i. However, this is the longest length of follow-up across all previous CVD-REAL studies, and is similar to recently published comparative effectiveness studies with a smaller cohort of patients, with findings consistent with ours [24–26]. Longer term follow-up would be informative to evaluate the outcomes over time.
Conclusion
The initiation of SGLT-2i as compared with other glucose-lowering drugs in routine clinical practice is associated with decreased risk of heart failure, all-cause death, myocardial infarction and stroke. The results of this large comparative effectiveness study with a broader, globally diverse population complement and extend the findings of completed randomized controlled trials.
Supplementary Information
Acknowledgements
The authors acknowledge Kevin Kennedy (Saint Luke's Mid America Heart Institute) for his independent validation of the meta analyses.
Fabian Hoti, Solomon Christopher and Minna Vehkala (StatFinn & EPID Research, Espoo, Finland) and Bendix Carstensen (Diabetes Center, Gentofte, Denmark) are all acknowledged for database management and statistical work.
Data from the Norwegian Patient Register have been used in this publication. The interpretation and reporting of these data are the sole responsibility of the authors, and no endorsement by the Norwegian patient register is intended nor should be inferred.
KK is supported by the National Institute for Health Research (NIHR) Applied Research Collaboration East Midlands (ARC EM) and the NIHR Leicester Biomedical Research Centre (BRC).
Editorial support in styling, formatting and submission of the manuscript was provided by Nicola Truss, PhD, inScience Communications, Springer Healthcare Ltd, UK, and funded by AstraZeneca.
Abbreviations
Authors’ contributions
PF, MT and MK contributed to the development of the study concept and design, data collection and analysis, interpretation of the data, and writing of the manuscript. KK contributed to the data collection, interpretation of the data, and writing of the manuscript. DJK, SK, CSPL, S-YG, C-EC, JS, MAC, NT, JF-N, RWH, MEJ, AN, JGE, FZ, AK, DM, HC, EW, JB, and FS, contributed to the data collection, interpretation of the data, and critical review and revision of the manuscript. All authors provided their final approval and agree to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriate investigated and resolved. All authors read and approved the final manuscript.
Funding
This study was funded by AstraZeneca. Some authors are employees of AstraZeneca; their contribution to the study design and to collection, analysis and interpretations of the data and in writing the manuscript is stated above.
Availability of data and materials
Data underlying the findings described in this manuscript may be obtained in accordance with AstraZeneca’s data sharing policy described at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure↗.
Declarations
Ethics approval and consent to participate
Informed consent was not required, as the data were collected for clinical and administrative purposes and were analysed after de-identification. Analyses of data were conducted in accordance with local laws and regulations, and received approvals from Scientific/Ethics/Data Protection Committees in each country. Country-specific analyses were conducted by independent academic/statistical groups in each country.
Consent for publication
Not applicable.
Competing interests
KK reports grants from AstraZeneca, during the conduct of the study; grants from Amgen, grants from AstraZeneca, grants from Bayer, grants from NAPP, grants from Lilly, from Merck Sharp & Dohme, personal fees from Novartis, personal fees from Novo Nordisk, personal fees from Roche, personal fees from Berlin-Chemie AG/Menarini Group, personal fees from Sanofi-Aventis, personal fees from Servier, personal fees from Boehringer Ingelheim, grants from Pfizer, grants from Boehringer Ingelheim, grants from AstraZeneca, grants from Novartis, grants from Novo Nordisk, grants from Sanofi-Aventis, grants from Lilly, grants from Merck Sharp & Dohme, grants from Servier, outside the submitted work.
SK has received grants from Bayer Yakuhin and Daiichi Sankyo and consulting fees from Bayer Yakuhin, Bristol-Myers Squibb, and Pfizer.
CSPL has received research support from Boston Scientific, Bayer, Roche Diagnostics, AstraZeneca, Medtronic, and Vifor Pharma; has served as consultant or on the Advisory Board/ Steering Committee/ Executive Committee for Abbott Diagnostics, Amgen, Applied Therapeutics, AstraZeneca, Bayer, Biofourmis, Boehringer Ingelheim, Boston Scientific, Corvia Medical, Cytokinetics, Darma Inc., Us2.ai, JanaCare, Janssen Research & Development LLC, Medtronic, Menarini Group, Merck, MyoKardia, Novartis, Novo Nordisk, Radcliffe Group Ltd., Roche Diagnostics, Sanofi, Stealth BioTherapeutics, The Corpus, Vifor Pharma and WebMD Global LLC; and serves as co-founder & non-executive director of Us2.ai.
MAC reports research support to his institution from Amgen, AstraZeneca, CSL Behring, GlaxoSmithKline, Novartis; consulting fees from Amgen, AstraZeneca, Bayer, Boehringer-Ingelheim, Boston Scientific, Edwards Lifesciences, Merck, Novo-Nordisk.
AN has received personal fees from AstraZeneca for this study, and honorarium for lectures and advisory board meetings for Novo Nordisk, Boehringer Ingelheim, and Lilly.
MEJ is a shareholder of Novo Nordisk. MEJ has received grants from AstraZeneca, Amgen, Boehringer Ingelheim and Sanofi Aventis.
RWH has received grants to his institution from AstraZeneca.
JF-N has received grants to his institution from AstraZeneca for this study and has received honoraria for lectures and consulting from Novartis, NovoNordisk, Sanofi, Lilly, Boehringer Ingelheim and Merck Sharp & Dohme.
NT has received consulting fees from Otsuka, Tricida, BI-Lilly, Janssen and AstraZeneca. He has received research support from AstraZeneca, Otsuka and Janssen, including for this work. He owns stock in Tricida, Pulsedata, Mesentech and Renibus. His research program is supported by the Canadian Institute for Health Research and Research Manitoba.
JES has received honoraria for advisory boards and lectures from AstraZeneca, Boehringer Ingelheim, Eli Lilly, Merck Sharp & Dohme, Mylan, Novartis, Novo Nordisk, Pfizer, and Sanofi.
AK has received grants and consulting fees from AstraZeneca, Novo Nordisk, Merck, and Boheringer Ingelheim.
S-YG has received institutional grants from AstraZeneca, Medtronic, and Sanofi. He has participated in advisory boards for Amgen, AstraZeneca, Boehringer Ingelheim, Novo Nordisk, Medtronic and Sanofi and has received honoraria for participation.
C-EC has received honorarium from AstraZeneca, Boehringer Ingelheim, Daiichi-Sankyo, MSD, Novartis, Pfizer, Sanofi.
JGE has received honorarium for lectures and advisory board meetings for Novo Nordisk, Boehringer Ingelheim, and AstraZeneca.
FZ has received honoraria for lectures from Napp Pharmaceuticals and Boehringer Ingelheim.
DM has received grants to her institution from AstraZeneca.
MT is an employee at Statisticon for which AstraZeneca is a client.
HC, EW, JS, FS and PF are AstraZeneca employees and hold stock options. JB is a AstraZeneca employee.
MK has received research grants from AstraZeneca and Boehringer Ingelheim, has served on advisory boards for AstraZeneca, Boehringer Ingelheim, Sanofi, Glytec, Novo Nordisk, ZS Pharma, Janssen, Merck (Diabetes) and Novartis; consultant for AstraZeneca, Boehringer Ingelheim, Sanofi, GSK, Janssen, Intarcia, Merck (Diabetes), Novo Nordisk, Glytec and ZS Pharma.
Footnotes
Contributor Information
Kamlesh Khunti, Email: kk22@leicester.ac.uk.
the CVD-REAL Investigators and Study Group:
Mikhail Kosiborod↗, Matthew A. Cavender↗, John P. Wilding↗, Kamlesh Khunti↗, Anna Norhammar↗, Kåre Birkeland↗, Marit Eika Jørgensen↗, Reinhard W. Holl↗, Carolyn S. P. Lam↗, Hanne Løvdal Gulseth↗, Bendix Carstensen↗, Esther Bollow↗, Josep Franch-Nadal↗, Luis Alberto García Rodríguez↗, Avraham Karasik↗, Navdeep Tangri↗, Shun Kohsaka↗, Dae Jung Kim↗, Jonathan Shaw↗, Suzanne Arnold↗, Su-Yen Goh↗, Chern-En Chiang↗, Johan G. Eriksson↗, Francesco Zaccardi↗, Peter Fenici↗, Johan Bodegård↗, Hungta Chen↗, Filip Surmont↗, Rachel Kendrick↗, Wesley Belli↗, Eric T. Wittbrodt↗, Matthias Saathoff↗, Yusuke Noguchi↗, Donna Tan↗, Maro Williams↗, Hye Won Lee↗, Maya Greenbloom↗, Oksana Kaidanovich-Beilin↗, Karolina Andersson-Sundell↗, Khung Keong Yeo↗, Yong Mong Bee↗, Joan Khoo↗, Agnes Koong↗, Yee How Lau↗, Fei Gao↗, Wee Boon Tan↗, Hanis Abdul Kadir↗, Kyoung Hwa Ha↗, Jinhee Lee↗, Gabriel Chodick↗, Cheli Melzer Cohen↗, Reid Whitlock↗, Lucia Cea Soriano↗, Oscar Fernándex Cantero↗, Jordan A. Menzin↗, Matthew Guthrie↗, Jennie Ilomaki↗, Dianna Magliano↗, Fabian Hoti↗, Solomon Christopher↗, and Minna Vehkala↗
References
Associated Data
Supplementary Materials
Data Availability Statement
Data underlying the findings described in this manuscript may be obtained in accordance with AstraZeneca’s data sharing policy described at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure↗.